Concepedia

Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2

Ethylin Wang Jabs, Xiang Li, Alan F. Scott, Gregory F. Meyers, Wendy Chen, Michael R. Eccles, Jen-i Mao, Lawrence Charnas, Charles E. Jackson, Michael Jaye

Nature Genetics · 1994 · 472 citations · 17 references

DOI

Concepts

References

17

Fluorescence detection in automated DNA sequence analysis

Lloyd M. Smith, Jane Z. Sanders, Robert Kaiser et al. · Nature · 1986 · 1.7K citations

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Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

Rita Shiang, Leslie M. Thompson, Yazhen Zhu et al. · Cell · 1994 · 1.3K citations

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Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome

William Reardon, Robin M. Winter, Paul Rutland et al. · Nature Genetics · 1994 · 768 citations

, , +6

Determination of ligand-binding specificity by alternative splicing: two distinct growth factor receptors encoded by a single gene.

Toyokazu Miki, Donald P. Bottaro, Timothy P. Fleming et al. · Proceedings of the National Academy of Sciences · 1992 · 757 citations

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[16] Splice junctions, branch point sites, and exons: Sequence statistics, identification, and applications to genome project

Periannan Senapathy, Marvin B. Shapiro, Nomi L. Harris · Methods in enzymology on CD-ROM/Methods in enzymology · 1990 · 686 citations

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